ClinVar
|
Risk
|
rs1057519927(C;C) rs1057519927(G;G) rs1057519927(T;T) |
Alt
|
rs1057519927(C;C) rs1057519927(G;G) rs1057519927(T;T) |
Reference
|
Rs1057519927(A;A) |
Significance |
Probable-Pathogenic |
Disease |
Neoplasm of breast Adenocarcinoma of prostate Transitional cell carcinoma of the bladder Uterine cervical neoplasms Small cell lung cancer Papillary renal cell carcinoma Adenocarcinoma of stomach Hepatocellular carcinoma Glioblastoma Adenocarcinoma of lung Oesophageal carcinoma Colorectal Neoplasms Malignant neoplasm of body of uterus Squamous cell carcinoma of lung Neoplasm of brain Squamous cell carcinoma of the head and neck |
Variation | info |
---|
Gene |
PIK3CA |
CLNDBN |
Neoplasm of breast Adenocarcinoma of prostate Transitional cell carcinoma of the bladder Uterine cervical neoplasms Small cell lung cancer Papillary renal cell carcinoma, sporadic Adenocarcinoma of stomach Hepatocellular carcinoma Glioblastoma Adenocarcinoma of lung Oesophageal carcinoma Colorectal Neoplasms Malignant neoplasm of body of uterus Squamous cell carcinoma of lung Neoplasm of brain Squamous cell carcinoma of the head and neck |
Reversed |
0 |
HGVS |
NC_000003.11:g.178936083A>C; NC_000003.11:g.178936083A>G; NC_000003.11:g.178936083A>T |
CLNSRC |
|
CLNACC |
RCV000417967.1, RCV000419304.1, RCV000420824.1, RCV000421246.1, RCV000421834.1, RCV000426519.1, RCV000426815.1, RCV000428636.1, RCV000430621.1, RCV000432777.1, RCV000437064.1, RCV000438048.1, RCV000438466.1, RCV000439966.1, RCV000441350.1, RCV000441904.1, RCV000418283.1, RCV000422972.1, RCV000423223.1, RCV000423683.1, RCV000425192.1, RCV000425864.1, RCV000428975.1, RCV000430389.1, RCV000434370.1, RCV000434554.1, RCV000435067.1, RCV000436379.1, RCV000440193.1, RCV000442566.1, RCV000442694.1, RCV000443286.1, RCV000418134.1, RCV000419045.1, RCV000420027.1, RCV000426905.1, RCV000427245.1, RCV000427440.1, RCV000427928.1, RCV000428899.1, RCV000432513.1, RCV000433205.1, RCV000435311.1, RCV000438103.1, RCV000438605.1, RCV000439562.1, RCV000442409.1, RCV000443002.1, |